Natco Pharma Limited
FDA inspection history in Rangareddy, India, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Rangareddy, India.
Cited most
Across all Natco Pharma Limited observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Natco Pharma Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Rangareddy, India
One Form 483 · 2019 · 6 observations
Latest: Form 483, Aug 9, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-09 | 483 Form 483 | Rangareddy, India | 6 | $99 |
Investigators on these documents
FEI number 3004065860 · most recent document Aug 9, 2019
About Natco Pharma Limited
How many FDA Form 483s has Natco Pharma Limited received?
FDA Intel has 1 Form 483 on file for Natco Pharma Limited; the most recent is dated Aug 9, 2019.
When was Natco Pharma Limited last inspected by FDA?
The most recent FDA inspection document on file for Natco Pharma Limited is a Form 483 dated Aug 9, 2019, for the site in Rangareddy, India.
What did FDA cite at Natco Pharma Limited?
The regulations cited most in the observations on file for Natco Pharma Limited are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.